flumazenil has been researched along with BH4 Deficiency in 6 studies
Flumazenil: A potent benzodiazepine receptor antagonist. Since it reverses the sedative and other actions of benzodiazepines, it has been suggested as an antidote to benzodiazepine overdoses.
flumazenil : An organic heterotricyclic compound that is 5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine which is substituted at positions 3, 5, 6, and 8 by ethoxycarbonyl, methyl, oxo, and fluoro groups, respectively. It is used as an antidote to benzodiazepine overdose.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 5 (83.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Takarada, Y | 2 |
| Yamashita, K | 2 |
| Kalanin, J | 2 |
| Kagawa, S | 2 |
| Matsuoka, A | 2 |
| Ohtsuka, N | 1 |
| Desviat, LR | 1 |
| Pérez, B | 1 |
| Ugarte, M | 1 |
| Feráková, E | 1 |
| Ferák, V | 1 |
| Kádasi, L | 1 |
| Poláková, H | 1 |
| Hejcmanová, L | 1 |
| Pijacková, A | 1 |
| Kalaydjieva, L | 1 |
| Kremensky, I | 1 |
| Tyfield, LA | 1 |
| Meredith, AL | 1 |
| Osborn, MJ | 1 |
| Harper, PS | 1 |
6 other studies available for flumazenil and BH4 Deficiency
| Article | Year |
|---|---|
[Genetic diagnosis of phenylketonuria. IV. Mutations of phenylalanine hydroxylase gene in Caucasian and Gypsy populations in Czech and Slovakia Republics].
Topics: Base Sequence; Czech Republic; Female; Genetics, Population; Humans; Male; Molecular Sequence Data; | 1994 |
Gypsy phenylketonuria: a point mutation of the phenylalanine hydroxylase gene in Gypsy families from Slovakia.
Topics: Adolescent; Adult; Base Sequence; Blotting, Southern; Child; Child, Preschool; DNA Mutational Analys | 1994 |
Phenylketonuria in Spanish Gypsies: prevalence of the IVS10nt546 mutation on haplotype 34.
Topics: Haplotypes; Heterozygote; Homozygote; Humans; Mutation; Phenylketonurias; Roma; Spain | 1997 |
A unique RFLP haplotype at the phenylalanine hydroxylase locus in Czechoslovak Gypsies with phenylketonuria.
Topics: Chromosome Mapping; Czechoslovakia; Female; Haplotypes; Humans; Male; Phenylalanine Hydroxylase; Phe | 1992 |
Screening for phenylketonuria in a totalitarian state.
Topics: Academies and Institutes; Attitude to Health; Bulgaria; Communism; Comprehension; Galactosemias; Hea | 1992 |
Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of Wales.
Topics: Alleles; Child; Consanguinity; DNA; DNA Probes; Ethnicity; Female; Haplotypes; Humans; Male; Mutatio | 1989 |